Hereditary transthyretin amyloidosis caused by p.Ser43Asn variant. A new endemic variant in Ecuador-Reference-Cited by-同舟云学术

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Hereditary transthyretin amyloidosis caused by p.Ser43Asn variant. A new endemic variant in Ecuador

Published:2023-07 Issue:7 Volume:76 Page:564-566
ISSN:1885-5857
Container-title:Revista Española de Cardiología (English Edition)
language:en
Short-container-title:Revista Española de Cardiología (English Edition)

Author:

Porres-López Elena,de Frutos Fernando,Silva-Hernández Lorenzo,Galán Lucía,González-López Esther,García-Pavía Pablo

Publisher

Elsevier BV

Subject

General Medicine

Reference6 articles.

1. Transthyretin amyloid cardiomyopathy;Garcia-Pavia;Med Clin (Barc).,2021

2. Characterization of hereditary transthyretin cardiac amyloidosis in Spain;Álvarez Rubio;Rev Esp Cardiol.,2022

3. Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases

4. detection of a rare case of familial cardiac amyloidosis (Ser23asn): Case report with literature review;Daoko;Rep Med Imaging.,2010

5. Technetium pyrophosphate myocardial uptake and peripheral neuropathy in a rare variant of familial transthyretin (TTR) amyloidosis (Ser23Asn): A case report and literature review;Castaño;Amyloid.,2012

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Histological Typing in Patients With Cardiac Amyloidosis;Journal of the American College of Cardiology;2024-03

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